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BMC Fam Pract. 2006; 7: 4.
Published online 2006 January 23. doi:
10.1186/1471-2296-7-4.
Copyright
[copyright] 2006 de la Jara et al; licensee BioMed Central Ltd.
Female asylum seekers with musculoskeletal pain: the
importance of diagnosis and treatment of hypovitaminosis D
G de Torrente de la Jara, 1 A
Pecoud,1 and B Favrat1
1Medical Outpatient Clinic, University of
Lausanne, Switzerland
Received July 20, 2005; Accepted January 23, 2006.
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Background
Hypovitaminosis D is
well known in different populations, but may be under diagnosed in certain
populations. We aim to determine the first diagnosis considered, the
duration and resolution of symptoms, and the predictors of response to
treatment in female asylum seekers suffering from hypovitaminosis D.
Methods
Design: A pre- and
post-intervention observational study.
Setting: A network comprising an academic primary care centre and nurse
practitioners.
Participants: Consecutive records of 33 female asylum seekers with
complaints compatible with osteomalacia and with hypovitaminosis D (serum
25-(OH) vitamin D <21 nmol/l).
Treatment intervention: The patients received either two doses of
300,000 IU intramuscular cholecalciferol as well as 800 IU of
cholecalciferol with 1000 mg of calcium orally, or the oral treatment
only.
Main outcome measures: We recorded the first diagnosis made by the
physicians before the correct diagnosis of hypovitaminosis D, the duration
of symptoms before diagnosis, the responders and non-responders to
treatment, the duration of symptoms after treatment, and the number of
medical visits and analgesic drugs prescribed 6 months before and 6 months
after diagnosis.
Tests: Two-sample t-tests, chi-squared tests, and logistic
regression analyses were performed. Analyses were performed using SPSS
10.0.
Results
Prior to the discovery
of hypovitaminosis D, diagnoses related to somatisation were evoked in 30
patients (90.9%). The mean duration of symptoms before diagnosis was 2.53
years (SD 3.20). Twenty-two patients (66.7%) responded completely to
treatment; the remaining patients were considered to be non-responders.
After treatment was initiated, the responders' symptoms disappeared
completely after 2.84 months. The mean number of emergency medical visits
fell from 0.88 (SD 1.08) six months before diagnosis to 0.39 (SD 0.83)
after (P = 0.027). The mean number of analgesic drugs that were prescribed
also decreased from 1.67 (SD 1.5) to 0.85 (SD 1) (P = 0.001).
Conclusion
Hypovitaminosis D in
female asylum seekers may remain undiagnosed, with a prolonged duration of
chronic symptoms. The potential pitfall is a diagnosis of somatisation.
Treatment leads to a rapid resolution of symptoms, a reduction in the use
of medical services, and the prescription of analgesic drugs in this
vulnerable population.
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Deficiency of vitamin D, leading to osteoporosis and osteomalacia, is
well known in elderly people in Western countries. A European survey in
community dwellers over 70 years showed hypovitaminosis D (25- [OH]
vitamin D <30 nmol/l) in 36% of men and 47% of women [1].
Hypovitaminosis D and osteomalacia have also been reported in the
immigrant Indo-Asian population in the UK since the 1960's [2-5].
Yet this disorder remains widely underconsidered according to more recent
studies, with one reporting a mean period of 59.2 months of complaints
before the diagnosis was established [6],
and another reporting a prevalence of 78% of hypovitaminosis D (versus 58%
in controls) in an Indo-Asian population attending a rheumatology clinic
in the UK [7].
A recent study in the United States showed that of 150 consecutive
patients (immigrant and non-immigrant) of a community clinic with
persistent, non-specific musculoskeletal pain, 100% had vitamin D
insufficiency (<50 nmol/l) and 28% had severe deficiency (<20
nmol/l) [8].
We have also previously reported eleven cases of symptomatic
hypovitaminosis D in female asylum seekers [9].
The condition has also been assessed in consecutively admitted medical
inpatients: 57% were considered vitamin D deficient (<37.5 nmol/l), of
whom 22% were severely deficient (<20 nmol/l) [10].
Finally, in recent years, several studies have examined the prevalence
of hypovitaminosis D in healthy subjects [11-13].
In the late winter months, it appears that 36% of young healthy adults in
Boston suffer from the condition (25-(OH) vitamin D <50 nmol/l) [13]
as well as 34% of healthy adults in Brussels (25-(OH) vitamin D <40
nmol/l) [12].
Thus, the disease is more prevalent than we generally suspect, not only
in at-risk individuals in our multicultural societies, but probably also
in a population that appears less vulnerable.
Concerning treatment, the benefit of the prophylactic use of vitamin D
and calcium has been established in Asian immigrants in the UK [14],
as well as in elderly subjects in regard to its effect on fractures and
falls [15,16].
Hardly any studies have measured the impact or clinical response to
treatment over time in a younger immigrant population. We are aware of one
study, on osteomalacic myopathy in veiled Arabic women in Denmark with a
mean age of 32.2 years, that demonstrated a normalisation of muscle
strength (except in maximal voluntary contraction) at 6 months after
initiation of treatment [17].
The purpose of the study was to assess the impact of diagnosis and
treatment in female asylum seekers with hypovitaminosis D. We first noted
the diagnosis made by the primary care physicians, as well as the delay in
the establishment of the diagnosis of hypovitaminosis D. We then assessed
the response to treatment by these parameters: improvement of clinical
symptoms (bone pain, muscle weakness, and fatigue), variation in the
number of analgesic drugs prescribed, and number of medical visits before
and after treatment.
Concerning the response to treatment, no predictors have yet been
defined. We therefore tried to extract from our study variables such as
age, length of stay in Switzerland, number of chronic illnesses, and
existence of psychiatric comorbidity as possible predictors of a positive
response to treatment.
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Patients
The study investigated
female asylum seekers attending an academic primary care centre serving a
population of 100,000 between March 2000 and April 2002. All of the
patients belong to a health network with a nurse practitioner gate-keeping
system and primary care physicians. The patients must always consult
within this setting and cannot change their primary care physician without
informing the nurse practitioner. After a certain number of cases of
hypovitaminosis D were diagnosed in 2000, the centre's primary care
physicians were informed by two circular letters, in March and April 2001,
of the suspected high prevalence of this disease in female asylum seekers,
particularly those with a minimal exposure to sunlight and presenting with
a history of bone pain, proximal muscular weakness, a change in gait
and/or fatigue. In suspected cases seen within the outpatient department
(emergencies and follow-ups), we checked serum levels of 25-(OH) vitamin
D, while the physician determined other biochemical parameters if judged
necessary: calcium, phosphate, alkaline phosphatase, and parathyroid
hormone (PTH). We included women with symptoms of hypovitaminosis D and a
confirmed deficiency in the study. Only women were included because of
their risk factors and histories. There were no exclusion criteria. In our
setting, we did not constitute a control group. The physicians were asked
several times to report their cases, but we did not revise all files
systematically. The physicians were advised to follow treatment
recommendations specified in the circular letters (300,000 IU of
intramuscular cholecalciferol with an ongoing course of 800 IU of
cholecalciferol associated with 1000 mg of calcium), but were free not to
do so. Therefore, the decisions to dose 25-(OH) vitamin D, to report the
cases, and to treat, if necessary, the patients, were left to the
physicians who were directly in charge of the patients. Nevertheless, we
discussed the two circular letters extensively with the primary care
physicians and had informal discussions as well.
No approval from a ethics committee was required for this study.
Indeed, in Switzerland, a chart review does not need an ethical committee
acceptance. All the patients included in the study gave their consent
concerning the treatment that is appropriate for hypovitaminosis D.
Furthermore, the physicians were free to follow treatment
recommendations.
Study design and treatment
The study
was a prospective observational study. Guidelines for treatment were
suggested in the circular letters and the majority of patients received
two intramuscular injections of 300,000 IU of cholecalciferol at monthly
intervals, as well as an ongoing course of oral calcium (1000 mg) and
cholecalciferol (800 IU = 20 [mu]g). After 6 months follow-up, we reviewed
the medical and nurse practitioner records to determine the main outcomes.
There was no standardized questionnaire designed for the follow-up. The
information was retrieved from the files with an extraction sheet only.
25-(OH) vitamin D was measured by a radioimmunoassay (RIA) with an
125I-labelled tracer (DiaSorin Inc.). Calcium and phosphate
levels were measured by spectrophotometry (Roche). The reference ranges
are 21 --131 nmol/l for 25-(OH) vitamin D, 2.15 --2.55 mmol/l for calcium
and 0.8 -- 1.6 mmol/l for phosphate. (For 25-(OH) vitamin D, 1 [mu]g/l =
2.5 nmol/l). The reference range for 25-(OH) vitamin D is derived from a
group of 20 male and 24 female healthy, predominately Caucasian volunteers
from the midwestern USA, aged between 23 and 67 years, during the month of
October (DiaSorin Inc.). It is well known, however, that this reference
range describes a severe hypovitaminosis D, and that levels below 50
nmol/l are considered insufficient (see Discussion section).
Outcomes
We determined a number of
parameters, including region of origin, length of stay in Switzerland,
first diagnosis, number of months prior to diagnosis, number of chronic
illnesses, psychiatric comorbidity, number of visits and emergency visits
six months before and six months after diagnosis, number of analgesic
drugs prescribed 6 months before and 6 months after diagnosis, resolution
of symptoms after treatment (we defined two categories: complete
resolution of symptoms as responders and partial or no resolution as
non-responders) and duration of resolution (partial or complete).
Statistics
Two-sample
t-tests, chi-squared tests, and logistic regression analyses were
performed. Analyses were performed using SPSS 10.0.
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The study population comprised 18 (54.5%) Somali women, 12 (36.4%)
Balkan women, and 3 (9.1%) women of other origin. The mean age was 38.8
years (SD 16.9). Twenty-three (69.7%) of the women wore a veil (partial or
complete, including gloves), and no corresponding details were available
for 2 patients (6.1%). The population had been residing in Switzerland for
a mean period of 5.27 years (SD 3). The patients were suffering from a
mean of 2.76 chronic illnesses, such as, iron deficiency with or without
anaemia, obesity, gastritis, tension headache, and hypertension (SD 1.97),
and 10 patients (30.3%) were considered to have one or more psychiatric
diagnoses other than somatisation.
The first diagnoses, before hypovitaminosis D was considered, were
chronic back pain, generally associated with pelvic or rib pain, in 17
patients (51.5%); somatisation disorder in 7 patients (21.2%); and
multiple unexplained somatic symptoms in 6 patients (18.2%). Regrouping
these different diagnoses, we obtain a total of 90.1% of patients with an
initial diagnosis related to somatisation. In 3 patients (9.1%), the
diagnosis of hypovitaminosis D was mentioned initially. The physicians
treating these 3 new patients had been formerly informed of the possible
high prevalence of the disease prior to the consultation and had suspected
it on presentation.
The mean duration of symptoms before diagnosis was 2.53 years (SD
3.20). The duration of symptoms after seeing a physician in our centre was
1.87 years (SD 2.20). Nevertheless, in retrospect, the majority of
complaints were quite typical of hypovitaminosis D from the outset.
On diagnosis, the mean serum 25-(OH) vitamin D level was 11.32 nmol/l
(SD 4.55). Most of these measurements (87.9%, 29 patients) were made from
November to May, at a time when sunshine levels are low (latitude
46.3[deg]).
For 28 patients (84.8%), the mean blood calcium level on diagnosis was
2.17 mmol/l (SD 0.09), and 42.9% of these patients had hypocalcaemia
(<2.15), with a minimum of 1.92 mmol/l.
Phosphate concentrations were measured in 25 patients (75.7%), and the
mean level was 0.98 mmol/l (STD 0.31). Of these patients, 32% were
hypophosphataemic (<0.8) and none were hyperphosphataemic.
Treatment consisted only of calcium and cholecalciferol p.o. in 10
patients (30.3%). The remaining 23 received, in addition, the two
injections of cholecalciferol.
With regard to symptom resolution, 22 patients (66.7%) experienced
complete resolution and 11 (33.3%) presented either partial (n = 6) or no
resolution (n = 5). The beginning of symptom resolution in responders was
already noted at 1.47 months (SD 0.59), and resolution was complete at
2.84 months (SD 1.76). One patient required seven months of treatment to
be free from symptoms.
Three patients did not consult the primary care physician or the nurse
practitioner in relation to the symptoms of hypovitaminosis D after
initiation of treatment. They were considered to be responders to
treatment, since the medical facilities were totally accessible to them
and, on the two occasions on which they did consult the nurse, they did
not complain of their initial symptoms.
During the whole period preceding diagnosis, the patients received a
mean of 3.27 analgesic drugs (SD 2.28), compared to a mean of 1.67 (SD
1.51) during the 6 months before diagnosis. In the 6 months after
diagnosis and initiation of treatment, the number of analgesic drugs fell
to 0.85 (SD 1), (P = 0.001). Certain patients suffered from chronic
medical conditions (tension headache, osteoarthritis, irritable bowel
syndrome, migraine) requiring analgesic medication that did not vary
significantly over the 12-month period for which we analysed the data.
We analysed the follow-up visits and the emergency visits. Our centre
was open 24 hours a day, 7 days a week. After diagnosis, 27 patients
(81.8%) received a medical follow-up in our centre, 3 patients (9.1%)
changed physician after at least one medical visit, and the remaining 3
(9.1%) were followed up by the nurse practitioners. There was no
difference between the follow-up visits before and after diagnosis.
However, the emergency visits fell from 0.88 (SD 1.08) six months before
diagnosis to 0.39 (SD 0.83) six months after (P = 0.027).
In a univariate analysis we analysed age, length of stay in
Switzerland, number of chronic illnesses, psychiatric comorbidity,
presence of a veil, level of 25-(OH) vitamin D, and duration of symptoms
before diagnosis, in relation to the resolution of symptoms. None of these
variables was significant. According to our logistic regression analysis,
neither age, nor the number of chronic illnesses, nor the existence of
psychiatric comorbidity were predictors of the response to treatment.
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Our results suggest that hypovitaminosis D is still going undiagnosed
in immigrant women. Indeed, the first diagnosis evoked, in an often
psychologically difficult context, is one suggestive either of somatoform
disorder as described in the International Classification of Diseases,
10th revision [18]
or "somatisation" as defined in the study of Simon et al [19].
In this study, we refer particularly to the definition concerning patients
with psychological disorders who report multiple unexplained somatic
symptoms. Nevertheless, pain due to hypovitaminosis D is quite well
defined. It is felt in the bones, not in the joints. In general, it is
symmetrical, beginning in the lower back and then spreading to the pelvis,
upper legs, and ribs. The patients may also present with proximal muscle
weakness.
In our study, the complaints lasted for a considerable length of time,
with important psychosocial repercussions in an already vulnerable
population. This reflects the poor knowledge of hypovitaminosis D
prevalent in a group of Swiss primary care physicians, and confirms the
study by Nellen [6].
The impact of information is important, leading in our study to the
diagnosis of 33 new cases in a year and a half. We wish to emphasize the
importance of the diagnosis in a female Balkan population, a group in
which osteomalacia has not yet been formally described. Only one-third of
these patients wore a veil, so there is no direct correlation between
these two parameters. It is nevertheless possible that global sun exposure
(due to housebound status) is limited, and that dietary factors have an
influence in this population.
After treatment, subjective improvement was already present after a
mean of 1.47 months, and resolution was complete after a mean of 2.84
months, with complete resolution at a maximum of 7 months in all patients
who responded to treatment. The resolution of symptoms is known to occur
approximately between 3 and 6 months: 3 months for symptoms due to the
osteopathy [6]
and 6 months for the myopathy [17].
Our results also show a reduction in the use of medical services and
the prescription of analgesic drugs. These results should be considered
preliminary, because no control group was constituted. Nevertheless, these
two facts could be of primary importance. The reduction in emergency
visits, not necessarily linked to hypovitaminosis D, probably reflects a
general improvement in well-being, compared to periods when the patients
were suffering from chronic pain. This has not been evaluated, but there
may have been an improvement in psychological factors that elevated the
threshold for an emergency medical visit. Secondly, the reduction in the
prescription of analgesic drugs is probably paralleled by a reduction in
use, as all NSAIDs in Switzerland are obtained on prescription and the
population studied possesses limited financial resources, which limit its
access to over-the-counter drugs. The probable reduction in use also
reduces the potential harmful side effects, particularly those associated
with NSAIDs. The economic impact of these two results has not been
established, but is another interesting consideration.
In the studied population, we found very low levels of 25-(OH) vitamin
D, which is regarded as the best laboratory indicator of functional
vitamin D status [20].
Over the past few years, this status has been regaining considerable
attention. Vitamin D receptors are found not only in bone and muscle but
also in the breast, colon, prostate, immune system, brain, and probably
other tissues of the body. Vitamin D deficiency affects bone metabolism,
and results in osteoporosis and osteomalacia (or rickets, in children),
and evidence is now emerging that hypovitaminosis D has other important
adverse effects on health, such as increasing the risks of autoimmune
diseases, cancers, and other chronic affections [21-23].
A long-term study of 180,000 women showed that women taking 400 IU of
vitamin D daily had 40% less risk of developing MS than those who did not
[24].
The risks of prostate and colon cancer are lower if 25-(OH) vitamin D
levels are above 50 nmol/l [25-27].
In this context, the optimal levels of vitamin D for health benefits have
been subject to a number of discussions and studies. It is now widely
accepted that 25-(OH) vitamin D levels below 20 nmol/l are indicative of
severe deficiency [28].
Levels of at least 50 nmol/l [29],
and according to some authors, 78 nmol/l [30],
are necessary to prevent secondary hyperparathyroidism. Recent evidence
showed that calcium is malabsorbed and fracture risk increases at serum
levels below ~80 nmol/l [31].
A 25-(OH) vitamin D level between 80 and 125 nmol/l seems optimal for
general health [21,22,31].
Risk factors (reduced exposure to sunlight and strict vegetarian diet) [10,32,33]
must be minimized to achieve these concentrations. Nevertheless, these
risk factors are difficult to modify; even in Australia, the paradox of
hypovitaminosis D in a sunny country is emerging as a public health
problem [34].
The most cost-effective way to reach optimal levels of 25-(OH) vitamin D
is increasing UVB exposure, by exposing the hands, arms, and face, if
culturally acceptable and with caution in low latitudes, without sunscreen
for 5 --15 min between 1000 and 1500 h in the spring, summer, and fall for
individuals with type II and III skin. Diet does not provide high doses of
vitamin D, since very few foods contain it (oily fish being one) and
fortified food has not met public health expectations. Routine
supplementation could be the only effective way of preventing
hypovitaminosis D in the population described in our study, since it is
not likely that sun exposure habits and diet will change to any meaningful
extent. For example, a large educational campaign within the Asian
community of Rochdale, UK, between 1970 and 1980 only resulted in an
improvement of biochemical markers of vitamin D deficiency among the
children [35].
The benefits of treatment seem clear in our symptomatic vitamin D
deficient population, even though we only assessed them by direct
questioning and by indirect parameters, as it has been done in other
fields [36].
We did not have the set-up to evaluate treatment by costly or invasive
methods (dynamometer testing or bone biopsy). The use of vitamin D in
Asian immigrants in the UK has been assessed only with biochemical markers
[14],
demonstrating a response by serum levels of 25-(OH) vitamin D after oral
supplementation and no change in the levels of calcium, phosphate, and
alkaline phosphatase. But, as we have revealed, hypovitaminosis D concerns
a much wider population, including immigrants and non-immigrants, and
young and old. One very interesting study showed the effectiveness of an
annual megadose of intramuscular cholecalciferol (600,000 IU) in patients
with vitamin D deficiency. This therapy appears to be safe, even if
certain concerns, such as hypercalciuria, need to be examined. This
treatment could potentially be applied on a large scale [37].
Two recent meta-analyses concerning elderly people have shown that intakes
of >700 IU are necessary to decrease by approximately 25% (hip, NNT
45/non-vertebral, NNT 27) and 22% (NNT 15) the risk of fractures and
falls, respectively [15,16].
The present Recommended Daily Amounts (RDA) in the United States are 200
IU (5 [mu]g) daily for young adults, 400 IU (10 [mu]g) for those aged 51
--70, and 600 IU (15 [mu]g) daily for those over 71 years of age [38].
Generally, experts recommend a daily intake of 800 --1000 IU per day for
concrete benefits in health [39,40].
The mode and frequency of administration remain to be studied in different
populations.
In this small group of patients, the parameters studied (age, length of
stay in Switzerland, chronic illness, psychiatric co morbidity, veil, and
level of 25-(OH) vitamin D were not predictive of response or
non-response.
Our study clearly suffers from a number of limitations. First, the
study lacks a control group. Second, we do not know the number of patients
that were not included in the study because of failure of the physicians
to properly record the data. Third, we do not possess the complete
biochemical data for all the patients (alkaline phosphatase, PTH, and
albumin). Finally, the records can occasionally be imprecise in the
descriptions of symptoms and diagnoses.
In conclusion, in the context of resurgent scientific interest in
vitamin D, hypovitaminosis D must be considered in a symptomatic, female,
asylum-seeking population, to avoid prolonging the duration of chronic
symptoms and a potential misdiagnosis of somatisation. The impact of
treatment is beneficial, with a rapid resolution of symptoms and
reductions in both the use of medical services and the prescription of
analgesic drugs. Physicians should therefore be aware of the importance of
this disease and the impact of rapid diagnosis and treatment. Future
research will have to consider the need for routine supplementation in
this and other populations.
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|
 |
Figure
1
Biochemical results
(25-(OH) vitamin D and calcium) of patients at the time of
diagnosis. |
 |
Figure
2
Mean number of emergency
medical visits 6 months before and 6 months after
diagnosis. |
 |
Figure
3
Mean number of analgesic
drugs 6 months before and 6 months after
diagnosis. | |
|
|